Kan Peter, Walker Marion L, Drake James M, Kestle John R W
Department of Neurosurgery, Primary Children's Medical Center, University of Utah, Salt Lake City, Utah 84113, USA.
J Neurosurg. 2007 May;106(5 Suppl):347-9. doi: 10.3171/ped.2007.106.5.347.
Slit ventricle syndrome (SVS) is a delayed complication of shunt insertion and occurs only in children with slitlike ventricles after shunt placement. Although SVS appears to be related to early shunt placement, its predisposing factors are largely unknown.
Baseline data in 737 children who had received shunts were obtained from the databases of two previous clinical trials. Ventricular size before shunt placement and at the last routine follow up was measured using the frontooccipital horn ratio (FOHR). Ventricles with an FOHR less than or equal to 0.2 at follow up were classified as slitlike ventricles. A univariate analysis was performed on data obtained in children with more than 1 year of clinical and radiographic follow up to identify risk factors for developing slitlike ventricles. These results were entered into a multivariate analysis to identify independent predictors of slitlike ventricles. Two hundred forty-four children had more than 1 year of clinical and radiographic follow-up data. The 23 patients (9.4%) who developed slitlike ventricles had shunts inserted at a younger age (42 compared with 134 days, p = 0.09) and were more likely to have developed hydrocephalus secondary to infection (37.5%), head injury (25.0%), or aqueductal stenosis (22.2%). Slitlike ventricles were seen in 10.8% of patients with differential-pressure valves, 10.5% of patients with Delta valves, and 3.6% of patients with Orbis-Sigma valves (p = 0.007). Regression analysis supported the role of the valve type in developing slitlike ventricles.
Age at shunt insertion and valve type appear to be the modifiable risk factors for developing slitlike ventricles. If the authors of subsequent studies can further validate these conclusions, slow-draining valves and delayed shunt insertion might be used to decrease the incidence of slitlike ventricles and SVS.
裂隙脑室综合征(SVS)是分流术插入后的一种延迟并发症,仅发生于分流术后脑室呈裂隙状的儿童。尽管SVS似乎与早期分流术插入有关,但其诱发因素大多未知。
从两项先前临床试验的数据库中获取737例接受分流术儿童的基线数据。使用额枕角比(FOHR)测量分流术插入前及最后一次常规随访时的脑室大小。随访时FOHR小于或等于0.2的脑室被分类为裂隙状脑室。对有超过1年临床和影像学随访数据的儿童所获数据进行单因素分析,以确定发生裂隙状脑室的危险因素。将这些结果纳入多因素分析,以确定裂隙状脑室的独立预测因素。244例儿童有超过1年的临床和影像学随访数据。发生裂隙状脑室的23例患者(9.4%)分流术插入时年龄较小(42天对比134天,p = 0.09),且更可能继发于感染(37.5%)、头部损伤(25.0%)或导水管狭窄(22.2%)而发生脑积水。在使用压差阀的患者中,10.8%出现裂隙状脑室;使用Delta阀的患者中,10.5%出现裂隙状脑室;使用Orbis-Sigma阀的患者中,3.6%出现裂隙状脑室(p = 0.007)。回归分析支持瓣膜类型在发生裂隙状脑室中的作用。
分流术插入时的年龄和瓣膜类型似乎是发生裂隙状脑室的可改变危险因素。如果后续研究的作者能够进一步验证这些结论,或许可使用缓慢引流瓣膜和延迟分流术插入来降低裂隙状脑室和SVS的发生率。